54086-39-4

Basic information

• Product Name: 5-Phenylacridophosphin-10(5H)-one
• Synonyms: 5-Phenylacridophosphin-10(5H)-one
• CAS NO: 54086-39-4
• Molecular Formula: C₁₉H₁₃OP
• Molecular Weight: 288.28
• Mol File: 54086-39-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Phenylacridophosphin-10(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Phenylacridophosphin-10(5H)-one(54086-39-4)
• EPA Substance Registry System: 5-Phenylacridophosphin-10(5H)-one(54086-39-4)

Safety Data

• Hazardous Substances Data: 54086-39-4(Hazardous Substances Data)

Upstream product

• 1079-66-9 chloro-diphenylphosphine 
• 1696-17-9 N,N-diethylbenzamide 
• 59273-35-7 9-phenyl-9,10-dihydro-9-phosphaanthracene 
• 15309-64-5 5-chloro-5,10-dihydro-acridophosphine 
• 2572-40-9 (o-carboxyphenyl)diphenylphosphine oxide 
• 54086-38-3 10-Phenyl-9,10-dihydro-10-λ⁵-acridophosphin-9,10-dion 

Downstream Products

• 61279-12-7 10-methyl-5-phenyl-5,10-dihydro-acridophosphin-10-ol 
• 61279-19-4 10-(2,2-dimethyl-propyl)-5-phenyl-5,10-dihydro-acridophosphin-10-ol 
• 61279-18-3 10-(2,2-dimethyl-propyl)-5-oxo-5-phenyl-5,10-dihydro-5λ⁵-acridophosphin-10-ol 
• 59273-36-8 10-tert-butyl-5-phenyl-5,10-dihydro-acridophosphin-10-ol 
• 65523-16-2 10-(3-dimethylamino-propyl)-5-phenyl-5,10-dihydro-acridophosphin-10-ol 
• 65523-15-1 5,10-diphenyl-5,10-dihydro-acridophosphin-10-ol 
• 61279-17-2 5-oxo-5-phenyl-5,10-dihydro-5λ⁵-acridophosphin-10-ol 
• 20995-81-7 10-phenyl-acridophosphine 
• 59273-38-0 10-phenyl-10H-5,10-ethano-acridophosphine-11,12-dicarboxylic acid anhydride 
• 59273-37-9 10-tert-butyl-5-phenyl-5,10-dihydro-acridophosphine 
• 65523-20-8 10-hydroxy-5,10-dimethyl-5-phenyl-5,10-dihydro-acridophosphinium; iodide 
• 65523-18-4 10-hydroxy-5-methyl-5,10-diphenyl-5,10-dihydro-acridophosphinium; iodide 
• 65523-23-1 5-methyl-5,10-diphenyl-5,10-dihydro-acridophosphinium; iodide 
• 59590-82-8 9-phenyl-9,10-dihydro-9-phosphaanthracene 9-oxide 

Relevant articles and documents

Organic Electron Acceptors Comprising a Dicyanomethylene-Bridged Acridophosphine Scaffold: The Impact of the Heteroatom

Stable two-electron acceptors comprising a dicyanomethylene-bridged acridophosphine scaffold were synthesized and their reversible reduction potentials were efficiently tuned through derivatization of the phosphorus center. X-ray crystallographic analysis combined with NMR, UV/Vis, IR spectroscopic, and electrochemical studies, supported by theoretical calculations, revealed the crucial role of the phosphorus atom for the unique redox, structural, and photophysical properties of these compounds. The results identify the potential of these electron deficient scaffolds for the development of functional n-type materials and redox active chromophores upon further functionalization.